Integrated Conversion of Polyesters, CO <sub>2</sub> , and Glycerol via Ethylene Oxide‐Mediated Tandem Process

C Cong Luo Z Ziyu Cen W Weilong Wen (Beijing National Laboratory for Molecular Sciences Key Laboratory of Colloid and Interface and Thermodynamics Institute of Chemistry Chinese Academy of Sciences Beijing China) T Tianrui Bi Z Zhiye Ma (Beijing National Laboratory for Molecular Sciences Key Laboratory of Colloid and Interface and Thermodynamics Institute of Chemistry Chinese Academy of Sciences Beijing China) J Jun Ma J Junfeng Xiang (Center for Physicochemical Analysis Measurement Institute of Chemistry Chinese Academy of Sciences Beijing 100190 China) Q Qinglei Meng (Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS Research/Education Center for Excellence in Molecular Sciences, Center for Carbon Neutral Chemistry) H Huizhen Liu (Institute of Chemistry, Chinese Academy of Sciences , , ,) J Jianling Zhang (Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS Research/Education Center for Excellence in Molecular Sciences, Center for Carbon Neutral Chemistry) Z Zhimin Liu L Longfei Lin (Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS research/Education Center for Excellence in Molecular Sciences, Center for Carbon Neutral Chemistry, Institute of Chemistry) B Buxing Han (Institute of Chemistry, Chinese Academy of Sciences , , ,)

Abstract

Abstract The co‐conversion of poly(ethylene terephthalate) (PET), CO 2 , and renewable carbon resources offers a sustainable strategy for reducing plastic waste and carbon emissions, but remains challenging. Here, we develop a one‐pot cycloaddition–transesterification–glycolysis (CTG) tandem process to efficiently convert PET, CO 2 , and glycerol into bis‐hydroxyethyl terephthalate (BHET) and glycerol carbonate, achieving yields of 92% and 99%, respectively. The process begins with the cycloaddition of ethylene oxide and CO 2 in an ionic liquid, followed by transesterification with glycerol to produce glycerol carbonate and ethylene glycol. The in situ‐generated ethylene glycol participates in PET glycolysis to yield BHET catalyzed by zinc acetate. Kinetic studies, isotope labelling, and theoretical calculations reveal that ethylene oxide serves two functions: (i) swelling the PET matrix to enhance mass transfer and (ii) providing ethylene glycol. The synchronized kinetics of cycloaddition, transesterification, and glycolysis enable ethylene oxide to play both roles effectively, significantly accelerating PET depolymerization at mild temperatures.

Article Details

Volume / Issue Vol. 64, Issue 52
Published December 22, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (13)

C

Cong Luo

Z

Ziyu Cen

W

Weilong Wen

Beijing National Laboratory for Molecular Sciences Key Laboratory of Colloid and Interface and Thermodynamics Institute of Chemistry Chinese Academy of Sciences Beijing China

T

Tianrui Bi

Z

Zhiye Ma

Beijing National Laboratory for Molecular Sciences Key Laboratory of Colloid and Interface and Thermodynamics Institute of Chemistry Chinese Academy of Sciences Beijing China

J

Jun Ma

J

Junfeng Xiang

Center for Physicochemical Analysis Measurement Institute of Chemistry Chinese Academy of Sciences Beijing 100190 China

Q

Qinglei Meng

Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS Research/Education Center for Excellence in Molecular Sciences, Center for Carbon Neutral Chemistry

H

Huizhen Liu

Institute of Chemistry, Chinese Academy of Sciences , , ,

J

Jianling Zhang

Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS Research/Education Center for Excellence in Molecular Sciences, Center for Carbon Neutral Chemistry

Z

Zhimin Liu

L

Longfei Lin

Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS research/Education Center for Excellence in Molecular Sciences, Center for Carbon Neutral Chemistry, Institute of Chemistry

B

Buxing Han

Institute of Chemistry, Chinese Academy of Sciences , , ,